Results 211 to 220 of about 141,892 (269)

Deterministic quantum light emitters in DNA origami-engineered molecule-MoS₂ hybrids. [PDF]

Light Sci Appl
Li Z, Zhao S, Melchakova I, Erber E, Sikeler C, Watanabe K, Taniguchi T, Liedl T, Högele A, Baimuratov AS, Martynenko IV.   +10 more
europepmc   +1 more source

Detection of a Target Nucleic Acid by Ligation-Assisted Fluorescence Enhancement of a Peptide Nucleic Acid (PNA) Twin Probe via Disulfide Binding. [PDF]

Biopolymers
Ouchi Y, Ishii K, Sato Y, Imai Y, Matsui H, Ohtsuki T, Hakata Y, Shigeto H, Yamamura S, Kitamatsu M.   +9 more
europepmc   +1 more source

Study on the Inhibitory Effect of FOs on Advanced Glycation End Products (AGEs) Formation. [PDF]

Foods
Lyu Y, Wang H, Ye X, Ge Z, Mao W, Cai Z, Zhang X, Sun W, Yu X.   +8 more
europepmc   +1 more source

A (poly)Pro tip for preserving native disulfide connectivity during thiol-maleimide bioconjugation of disulfide-rich peptides. [PDF]

Chem Sci
Azzoug L, Novak A, Meudal H, Madinier JB, Charpentier S, Loth K, Morisset-Lopez S, Pifferi C, Aucagne V.   +8 more
europepmc   +1 more source

Thiol-Retaining N-Terminal Cysteine Chemistry for Dual Modification and Bicyclic Peptide Construction. [PDF]

J Am Chem Soc
Liu J, Duan S, Huang Y, Jian MY, Lee HS, Dai G, Wu C, Wu YL, Tsai YH.   +8 more
europepmc   +1 more source

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Thiol groups in hemocyanins

Comparative Biochemistry and Physiology, 1965
Abstract 1. 1. The total sulfhydryl groups and the number of free SH groups of hemocyanins from different sources has been determined. Hemocyanins are well characterized by their content of “half cystine”, much more than by the content of any other amino acid. 2. 2.
A, Ghiretti-Magaldi, C, Nuzzolo
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On the Reactivity of the Thiol Group of Thiolsubtilisin

European Journal of Biochemistry, 1973
The reaction of thiolsubtilisin with iodoacetamide shows that in the alkaline pH‐range the –SH group of the enzyme reacts like a simple thiol compound such as mercaptoacetate. On the other hand, around neutral pH the enzyme displays enhanced reactivity compared with that of mercaptoacetate.
László Polgár, Piroska Halász, Ernó Moravcsik   +2 more
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Thiol Groups and Morphogensis

Nature, 1959
WE have recently shown1,2 that β-mercaptoethanol (a strongly reducing –SH-containing substance) markedly inhibits morphogenetic movements (gastrulation, closure of neural plate) in amphibian eggs. The oxidized counterpart of β-mercaptoethanol (dithiodiglycol) produces a thickening of the neural plate; the same type of abnormalities can be obtained with
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